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5+ years of experience working with EDC clinical software solutions in end-to-end data management related activities (database design, data collection, data analysis, query resolution, datasets, statistical reporting.
$80,000 - $200,000 a yearRemoteExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Enhanced by state-of-the-art lighting, pyrotechnics and sound design, large-scale art installations, theatrical performers and next generation special effects, our events captivate the senses and inspire a unique level of fan interaction.
$16 - $20 an hourPart-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Experience using computer applications including spreadsheets, email, word-processing software & web-based systems (EDC, IVR/IWRS, CTMS). Experience using computer applications including spreadsheets, email, word-processing software & web-based systems (EDC, IVR/IWRS, CTMS.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Master Data Management, Regulatory, Quality, OpenData, Safety, R&D, Study Startup, Clinical Data Management, CTMS, Oncology Data, eTMF, Clinical Operations, Events Management, Territory Alignment , Multichannel CRM, Customer Reference Data, Cosmetics, Consumer Goods , Chemical, Animal Health , Remote Engage Meeting, Medical Devices, EDC, CDB, Vault Coder, Vault Payments, Vault QMS, Quality Docs, and Medcomms.
$85,000 - $225,000 a yearExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Administration skills a plusAzure Cloud Technologies: Azure Data Factory, Azure Databricks, Azure Blob Storage, Azure Data Lake, Azure Power Apps and Azure FunctionsCI/CD: GitHub, Jenkins, Azure DevOps, TerraformBI Analytics Tool Stack - Cognos, Tableau, Power BI, Alteryx, Denodo, and GrafanaData Wehousing: DataStage, InformaticaData Governance and Privacy: Informatica Axon and EDC, BigID.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Clinical research, Clinical trial, Pre-screening patients, EDC. Clinical research, Clinical trial, Pre-screening patients, EDC. The Research Assistant (RA) position delivers a strong customer experience for both sites and patients by providing virtual study support under the delegation of a PI. The RA is accountable for study delivery at the patient level and is expected to support the patient experience, data management, and other study administrative tasks with a quality-first approach.
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Excellent technical skills and ability to quickly learn new software; advanced MS Excel; preferred experience with Clinical Trial Management System (CTMS), and/or Site Payment platform, EDC and financial systems.
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This includes Source Data Validation (SDV) of clinical study data entered on the Case Report Forms (CRF) in the Electronic Data Capture (EDC) system, review and reconciliation of the Investigational Site File (ISF) with the Electronic Trial Master File (eTMF), ensure proper documentation of Investigational Product (IP), and ensure overall adherence to protocol procedures.
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Verify that trial data entered in the EDC is consistent with patient clinical notes and other source documentation (SDV). Monitor clinical trial progress, in conjunction with the AFT In-House Clinical Research Associate (IHCRA), through a combination of remote data review and remote/on-site monitoring visits.
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Solid understanding of the drug development process, including Good Clinical Practice (GCP) and FDA Code of Federal Regulations. The Clinical Research Monitor works in partnership with the AFT Project Manager and individual study teams to complete all site monitoring activities across assigned AFT projects and ensures all participating sites are compliant with Good Clinical Practice (GCP), SOPs, policies, and regulatory requirements throughout the life of assigned clinical trials.
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Act as a SME on core business software solutions (e.g., RAVE EDC system) to provide novel end-to-end software solutions that improve, automate, and solve complex business process challenges. Lead the development of clinical study databases in the Rave EDC system according to the department SOPs, including programming complex Custom Functions in C.
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Solid computer skills, proficient in MS Word and Excel; preferred experience using CTMS, EDC, or financial systems. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks forclinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
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Serves as the Lead Associate for administrative, reporting, contractual and financial support to the department related to the processing of payments to FSP investigative sites. We have a flexible working culture, where PPD clinical research services truly value a work-life balance.
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The Clinical Research Monitor will work under the Executive Director of Clinical Trial Operations and the Associate Director of Clinical Trial Operations to oversee activity at Alliance for Clinical Trials in Oncology sites participating in Alliance Foundation Trials (AFT) clinical trials.
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The incumbent will oversee outsourced studies ensuring appropriate interpretation and translation of the study protocol into validated data collection applications, tools, and systems (EDC, eCOA, IWRS), cleaning and validation of the data, and delivery of fit for use data for analyses.
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